Novel FABP4+C1q+ macrophages enhance antitumor immunity and associated with response to neoadjuvant pembrolizumab and chemotherapy in NSCLC via AMPK/JAK/STAT axis.

IF 8.1 1区 生物学 Q1 CELL BIOLOGY
Dong Zhang, Min Wang, Gen Liu, Xin Li, Wenwen Yu, Zhenzhen Hui, Xiubao Ren, Qian Sun
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引用次数: 0

Abstract

Immune checkpoint inhibitors (ICIs) immunotherapy facilitates new approaches to achieve precision cancer treatment. A growing number of patients with non-small cell lung cancer (NSCLC) have benefited from treatment with neoadjuvant ICIs combined with chemotherapy. However, the mechanisms and associations between the therapeutic efficacy of neoadjuvant pembrolizumab and chemotherapy (NAPC) and macrophage subsets are still unclear. We performed single-cell RNA sequencing (scRNA-seq) and identified a novel FABP4+C1q+ macrophage subtype, which exhibited stronger proinflammatory cytokine production and phagocytic ability. This subtype was found to be more abundant in tumor tissues and lymph nodes of major pathological response (MPR) patients compared to non-MPR patients, and was associated with a good efficacy of NAPC. Multiplex fluorescent immunohistochemical (mIHC) staining was subsequently used to verify our findings. Further mechanistic studies indicated that FABP4 and C1q regulate the expression of proinflammatory cytokines synergistically. In addition, FABP4 and C1q promote fatty acid synthesis, enhance anti-apoptosis ability and phagocytic ability of macrophage via the interaction of AMPK/JAK/STAT axis. This study provides novel insights into the underlying mechanisms and predictive biomarkers of NAPC. Our findings contribute to improving the prognosis of patients with NSCLC by potentially guiding more precise patient selection and treatment strategies. NOVELTY & IMPACT STATEMENTS: We identified a group of macrophages (FABP4+C1q+ macrophages) related to the therapeutic efficacy of neoadjuvant chemoimmunotherapy. FABP4+C1q+ macrophages highly expressed proinflammatory cytokines-related genes and had a strong cytokine production and phagocytic ability. We believe that our study provides a novel insight into the synergistic mechanism of neoadjuvant ICI combined with chemotherapy and may lead to improved clinical outcomes in patients with NSCLC in the future.

新型 FABP4+C1q+ 巨噬细胞通过 AMPK/JAK/STAT 轴增强抗肿瘤免疫力,并与 NSCLC 患者对新辅助治疗 pembrolizumab 和化疗的反应相关。
免疫检查点抑制剂(ICIs)免疫疗法是实现癌症精准治疗的新方法。越来越多的非小细胞肺癌(NSCLC)患者从新辅助 ICIs 联合化疗的治疗中获益。然而,新辅助彭博利珠单抗和化疗(NAPC)的疗效与巨噬细胞亚群之间的机制和关联仍不清楚。我们进行了单细胞 RNA 测序(scRNA-seq),发现了一种新型的 FABP4+C1q+ 巨噬细胞亚型,它具有更强的促炎细胞因子产生能力和吞噬能力。与非病理反应患者相比,该亚型在主要病理反应(MPR)患者的肿瘤组织和淋巴结中含量更高,并且与NAPC的良好疗效相关。随后,多重荧光免疫组化(mIHC)染色验证了我们的发现。进一步的机理研究表明,FABP4 和 C1q 能协同调节促炎细胞因子的表达。此外,FABP4 和 C1q 通过 AMPK/JAK/STAT 轴的相互作用,促进脂肪酸的合成,增强巨噬细胞的抗凋亡能力和吞噬能力。这项研究为了解 NAPC 的潜在机制和预测性生物标志物提供了新的视角。我们的研究结果可能会指导更精确的患者选择和治疗策略,从而有助于改善 NSCLC 患者的预后。新颖性和影响声明:我们发现了一组与新辅助化疗免疫疗法疗效相关的巨噬细胞(FABP4+C1q+巨噬细胞)。FABP4+C1q+ 巨噬细胞高度表达促炎细胞因子相关基因,并具有很强的细胞因子生成和吞噬能力。我们相信,我们的研究为新辅助 ICI 联合化疗的协同机制提供了一个新的视角,并可能在未来改善 NSCLC 患者的临床预后。
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来源期刊
Cell Death & Disease
Cell Death & Disease CELL BIOLOGY-
CiteScore
15.10
自引率
2.20%
发文量
935
审稿时长
2 months
期刊介绍: Brought to readers by the editorial team of Cell Death & Differentiation, Cell Death & Disease is an online peer-reviewed journal specializing in translational cell death research. It covers a wide range of topics in experimental and internal medicine, including cancer, immunity, neuroscience, and now cancer metabolism. Cell Death & Disease seeks to encompass the breadth of translational implications of cell death, and topics of particular concentration will include, but are not limited to, the following: Experimental medicine Cancer Immunity Internal medicine Neuroscience Cancer metabolism
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